1 / 24

IAQG 9120:2009 Revision Overview

IAQG 9120:2009 Revision Overview. Prepared by IAQG 9120 Team Rev: 2 Dated: 15 July 2009. Overview Objectives. Provide an overview of: 9120 Team Membership 9120 Revision Process 9120:2009 Key Changes (Revisions/Relocated, Additions, Deletions Requirements)

Patman
Download Presentation

IAQG 9120:2009 Revision Overview

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. IAQG 9120:2009 Revision Overview Prepared by IAQG 9120 Team Rev: 2 Dated: 15 July 2009

  2. Overview Objectives • Provide an overview of: • 9120 Team Membership • 9120 Revision Process • 9120:2009 Key Changes (Revisions/Relocated, Additions, Deletions Requirements) • 9120 Implementation Schedule

  3. 9120 Team Membership • 8 Members on 9120 Team • Representing: • Americas, Europe, and Asia-Pacific IAQG Sectors • Distributors, OEMsand Associations • Both Production andAftermarket

  4. 9120 Stakeholders • Civil Aviation Authorities • Defense Industry and Authorities • Space Industry and Authorities • Certification / Registration Bodies • Trade Associations • Suppliers • IAQG Member Companies • IAQG Strategy Streams and Teams

  5. 9120 Revision Objectives Incorporate ISO 9001:2008 changes Ensure alignment with IAQG strategy (on-time, on-quality performance) Align with IAQG 9100:2009 changes Adopt new requirements based on stakeholder needs Improve existing requirements where stakeholders identified need for clarification, including when a documented procedure is required

  6. 9120 Revision Process Project Mgmt Design Specification & IAQG Strategy > 9120 objectives • Started in Dec 2005 • 1st9120 Team Meeting • October 2006 Stakeholder Input Web survey Data mining and Consolidation - 84 items MCRT(Master Comments Review Template) • Review process  • Design Specification & IAQG Strategy > 9100 and 9120 objectives MCRTAccept/Reject/Proposals/ Comments 80 % accepted

  7. 9120 Revision Process 9120 draft 16 April 2007 Writing the first draft - prepared by the scribe 9120 draft 7 August 2007 Review of the first draft * IAQG Meeting - October 2007 • Review of Coordination Draft(Dec 2007) : • Stakeholder Comments Reviewed by: • Each Sector for consensus response • Entire team (in Naples) for final • resolutions prior to formal ballot 9120 coorddraft Nov 2007 * IAQG Meeting - April 2008

  8. 9120 Revision Process • Preparation for Formal Sector Ballot • Development of deployment support material • Formal Ballot • Jan 2009 • Limit date for comments • Mar 2009 9120 Formal Ballot Jan 2009 New ISO 9001 schedule(TC176 changed their estimated release date from June 2009 to October 2008) 9100 Revision Effort Completion: Dec 2008 AS/EN 9100 Publication: January 2009 AS/EN 9120 Publication: May 2009

  9. 9120:2009 Key Changes • Title – Distributors (removed “Stockist”) • Clause 1 - 9120 Scope and Application • Revision: • Scope extended to include Defense as well as Aviation and Space • Application guidance provided when 9100, 9110, and 9120 are appropriate for use • Rationale: • The 9120 based QMS is applicable to other complex systems and would receive benefit from implementation including land and sea based applications • Implementation/Audit Considerations: • Increased use and improved understanding of when the various aviation, space, and defense standards are applicable

  10. 9120:2009 Key Changes • Clause 3.3 & 3.7 – Counterfeit Part / Suspected Unapproved Part (SUP) • Addition:Define difference between counterfeit and unapproved parts in the supply chain • Counterfeit Parts are: • fraudulent • imitations of existing products • have no authority for use • SUPs are: • parts or products that have unknown authority or and may or may not be acceptable

  11. 9120:2009 Key Changes • Clause 3.5 - Risk • Addition: Define new term “risk” • An undesirable situation or circumstance that has both a likelihood of occurring and a potentially negative consequence • Rationale: The understanding of risk is importantfor an organization to develop a proactive quality management system • Implementation/Audit Considerations: • Understanding this term is important to implement a risk management process in the applicable clauses

  12. 9120:2009 Key Changes • Clause 4.1 – QMS General requirements • Revision/Relocation: • The organization’s QMS shall address customer and applicable statutory and regulatory QMS requirements (previously located in the QMS documentation § 4.2.1) • Rationale: • Clarify that the requirement is placed at the QMS level and not only at the documentation level • Implementation/Audit Considerations: • The concept of “basic QMS” may be used (processes applicable to all customers / activities), but the documents such as Quality Management Plans, which address specific customers requirements, shall be considered as part of the QMS

  13. 9120:2009 Key Changes • Clause 4.2.2 – Quality Manual Relationships • Deletion: • Requirement to create a document showing the relationship between 9120 requirements and the organizations documented procedures • Rationale: • Requirement adds no value to assuring product quality. • Requirement was viewed as prescriptive in that it specifies a particular method of assuring the requirements of the standard have been met • Implementation/Audit Considerations: • Auditors need to identify appropriate documented procedures as an inherent part of carrying out the audit

  14. 9120:2009 Key Changes • Clause 4.2.4 – Record Retention Requirement • Deletion: • Requirement to maintain records for 7 years min. • Rationale: • Conflicts with Regulatory / Customer requirements • Requirement was viewed as prescriptive in that it specifies a particular method of assuring the requirements of the standard have been met • Implementation/Audit Considerations: • Auditors need to identify appropriate record retention requirements per contracts as an inherent part of carrying out the audit

  15. 9120:2009 Key Changes • Clauses 5.2/8.2.1 – Customer Focus/Satisfaction • Addition: • Top management shall ensure that product conformity and on-time delivery performance are measured and that appropriate action is taken if planned results are not, or will not be, achieved. (5.2) • Information to be monitored and used for the evaluation of customer satisfaction shall include, but is not limited to: • product conformity • on-time delivery performance • customer complaints • corrective action requests • Organizations shall develop and implement plans for customer satisfaction improvement that address deficiencies identified by these evaluations, and assess the effectiveness of the results (8.2.1)

  16. 9120:2009 Key Changes • Clauses 5.2/8.2.1 – Customer Focus/Satisfaction (Continued) • Rationale: • Establish clear relationship between the QMS and organizational performance, in line with IAQG strategy • To promote continuous improvement of customer satisfaction • Implementation/Audit Considerations: • Review of management focus and organizational process to measure customer satisfaction and plan improvements

  17. 9120:2009 Key Changes • Clauses 7.1 – Planning of Product Realization • Addition: • This Clause is NOT EXCLUDED for Distributors • Rationale: • Distributors have a “product” (service) they provide • Controls and documents the need for product realization to be planned in addition to other requirements of the standard • Allows introduction of other considerations required by the industry (configuration management) • Implementation/Audit Considerations: • Clause 7.1 should be considered in any system assessment for a distributor

  18. 9120:2009 Key Changes • 7.1.1 / 7.5.3 - Configuration Management • Addition: • Deemed applicable to Distributors • Structured in line with ISO 10007 requirements • Rationale: • Focuses configuration management on the product and how it is sustained throughout product realization • Implementation/Audit Considerations: • Some level of configuration management is expected for all products at all levels of the supply chain in compliance with exclusion criteria (see clause 1.2)

  19. 9120:2009 Key Changes • 7.1.2 – Work Transfer • Addition: • The organization must have a process to plan and control the transfer activities • Expanded to cover permanent transfer (e.g. from one organization to another, from one organization to supplier, from one supplier to another) • Rationale: • Work transfer can occur at anytime during product realization • Addresses problems that often occur during work transfers • Implementation/Audit Considerations: • A process must exist to control the transfer of work including planning and subsequent control of the transfer

  20. 9120:2009 Key Changes • Clause 7.4.1 – Recognition of Supplier Quality Data • Revision: • Added note to recognize that one factor that may be used during supplier selection and evaluation is objective and reliable data from external sources • Rationale: • Recognition that the industry trend is to use externally provided supplier performance data (e.g. Online Aerospace Supplier Information System – OASIS, Nadcap) • Implementation/Audit Considerations: • Note only

  21. 9120:2009 Key Changes • Clause 7.4.1 – Approval status for suppliers • Revision: • Added and provided examples of “approval status” (e.g. approved, conditional, disapproved) and examples of “scope of approval” (e.g. product type, process family). • The organization must define the process for suppliers approval status decisions or changes • Rationale: • Clarify that the conditions for using a supplier depends on its approval status • Implementation/Audit Considerations: • The process, responsibilities and authority must be defined for this process

  22. 9100:2009 Key Changes • Clause 8.2.4 –Sampling Inspection • Revision: • When the organization uses sampling inspection as a means of product acceptance, the sampling plan shall be justified on the basis of recognized statistical principles and appropriate for use (i.e., matching the sampling plan to the criticality of the product and to the process capability) • Rationale: • Numerous requests were received to improve clause 8.2.4. The comments ranged from that it was statistically inaccurate, to that it was too prescriptive • Implementation/Audit Considerations: • Validation of recognized statistical principles utilized. • Process used to determine criticality of product

  23. Proposed 9120 Implementation Schedule Maximum 30 month Implementation from Publication 9120 Release + 18 Months + 3 Months + 30 Months 3 Months 12 Months 12 Months Develop Auditor Training Train Certification Bodiesand Auditors All Companies to Upgrade to New Standard At Next Surveillance Audit Or Re-Certification Earliest Opportunityfor Certification to New Standard (i.e. the early adopters) Maximum Allowed Time to Upgrade

  24. In Closing • The 9120 Team goals and objectives were to: • Align with IAQG 9100 and overall IAQG goals • Expand the 9120 scope to include Aviation, Space & Defense • Provide additional focus on IAQG objective of on-time and on-quality deliveries • Ensure 9120 standard is compatible for use by all stakeholder segments and by organizations of all types and sizes • Ensure 9120 stays recognized by authorities • Ensure extensive stakeholder involvement in revision effort by the use of a project management approach to solicit input and manage the revision The key changes are not inclusive of all the changes in the 9120 standard.

More Related